拉福拉病与衰和DM1一起出现:一个病例研究
Ramin Khanalizadeh1, Kosar Karimi2
1School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran.
Acta neurologica Taiwanica
|January 2, 2025
概括
本案例研究突出了拉福拉病,这是一种罕见的疾病,导致神经衰退. 早期诊断对于患有肌肉瘤和发展精神和小脑缺陷的儿童至关重要.
科学领域:
- 神经学 神经学
- 罕见的遗传疾病 罕见的遗传疾病
背景情况:
- 拉福拉病是一种罕见的,渐进的肌性.
- 它通常出现在童年或青春期.
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